Canonical Allele Identifier: CA2080454206
Gene: RPL21 HGNC NCBI

Linked Data

dbSNP Id: rs1881775457

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254107A>G , CM000675.2:g.27254107A>G GRCh38
NC_000013.10:g.27828244A>G , CM000675.1:g.27828244A>G GRCh37
NC_000013.9:g.26726244A>G NCBI36
NG_046927.1:g.7553A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.68-113A>G MANE Select ENSP00000346027.4:n.68-113A>G
ENST00000272274.8:c.68-113A>G ENSP00000351021.2:n.68-113A>G
ENST00000311549.10:c.68-113A>G ENSP00000346027.4:n.68-113A>G
ENST00000319826.8:c.68-113A>G ENSP00000370574.1:n.68-113A>G
ENST00000326092.8:c.68-113A>G ENSP00000370569.1:n.68-113A>G
ENST00000461690.5:c.68-113A>G ENSP00000434298.1:n.68-113A>G
ENST00000466550.1:n.80-113A>G
ENST00000473558.5:n.304-113A>G
ENST00000483765.5:c.67+264A>G ENSP00000473246.1:n.67+264A>G
ENST00000493317.1:c.68-113A>G ENSP00000471695.1:n.68-113A>G
NM_000982.3:c.68-113A>G NP_000973.2:n.68-113A>G
NM_000982.4:c.68-113A>G MANE Select NP_000973.2:n.68-113A>G